At a Glance
- Tasks: Lead upstream process development and ensure smooth tech transfers in a dynamic biotech environment.
- Company: Join Summit Therapeutics, a pioneering company focused on innovative therapies for cancer treatment.
- Benefits: Enjoy a collaborative culture, opportunities for growth, and the chance to make a real impact.
- Why this job: Be part of groundbreaking clinical trials and contribute to life-changing therapies for patients.
- Qualifications: Bachelor's degree with 8+ years experience in biotech or related fields; advanced degrees preferred.
- Other info: Work closely with cross-functional teams and external partners to drive project success.
The predicted salary is between 48000 - 72000 £ per year.
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Ivonescimab, known as SMT112, is a novel, potential first-in-class investigational bispecific antibody combining the effects of immunotherapy via a blockade of PD-1 with the anti-angiogenesis effects associated with blocking VEGF into a single molecule. Ivonescimab displays unique cooperative binding to each of its intended targets with multifold higher affinity when in the presence of both PD-1 and VEGF.
Summit has begun its clinical development of ivonescimab in non-small cell lung cancer (NSCLC), with three active Phase III trials:
HARMONi is a Phase III clinical trial which intends to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who have progressed after treatment with a 3rd generation EGFR TKI (e.g., osimertinib).
HARMONi-3 is a Phase III clinical trial which is designed to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC.
HARMONi-7 is a Phase III clinical trial which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC whose tumors have high PD-L1 expression.
Ivonescimab is an investigational therapy that is not approved by any regulatory authority in Summit’s license territories, including the United States and Europe. Ivonescimab was approved for marketing authorization in China in May 2024. Ivonescimab was granted Fast Track designation by the US Food & Drug Administration (FDA) for the HARMONi clinical trial setting.
Overview of Role:
The Manager, Upstream MSAT, is an enthusiastic process engineer who will work within a vibrant development environment as we approach the commercialization of our lead asset, Ivonescimab. The ideal candidate will have proven technical ability in the upstream production of biologics. The role involves working with the Summit MSAT group and other CMC, quality, and regulatory stakeholders in drug substance and product development to provide operational and technical oversight on all upstream-related activities across the organization and support the supply of required material/information to achieve Summit milestones. This position will require building operational relationships with Summit CDMOs and working in close collaboration internally and externally to ensure successful CMC deliverables.
Role and Responsibilities:
Contribute to and have accountability for all Summit CMC activities, focusing on the design of new or improved upstream processes and technical troubleshooting to support drug substance (DS) and product (DP) development, control strategies, specifications, etc.
Support phase-appropriate upstream process development, characterization, validation, and technology transfers to or between external CDMOs for drug substance (DS)
Assist in planning and execution of upstream activities
Assess and manage process risks arising from manufacturing or process changes
Develop effective working relationships with Summit project team members and external Contract Manufacturing Organizations (CMOs)
Assist in the generation, update, and/or review of regulatory filings
Support MSAT team objectives while providing clear and concise updates of results and reports to the project team leaders, including the Head of CMC
Work in close partnership with process scientists & engineers, QA, RA, supply chain, consultants, and cross-functionally
Support CMC sub-teams and programs
Facilitate problem-solving, contingency planning, and decision-making
Provide technical support to manufacturing operations, addressing and resolving any issues that arise during upstream processing
Drive continuous improvement to enhance process robustness, efficiency, and scalability.
Oversee tech transfer activities to ensure a seamless transition from development to manufacturing
Perform risk assessments to identify and mitigate potential issues in upstream processes.
Manage process deviation investigations and change controls
Travel as needed to support technology transfer, process scale-up, and collaboration with external partners
All other duties as assigned
Experience, Education and Specialized Knowledge and Skills:
Bachelor’s degree in chemical engineering, biotechnology, pharmaceutical science, or a related field with 8+ years of relevant experience; Master’s degree in chemical engineering, biotechnology, pharmaceutical science, or a related field with 6+ years of relevant experience; PhD in chemical engineering, biotechnology, pharmaceutical science, or a related field with 5+ years of relevant experience.
Demonstrated experience in process development, MSAT (Manufacturing Science and Technology), and/or manufacturing in a biological environment (preferably mAbs)
Proven technical knowledge in various bioreactor systems (e.g., Ambr15/250, Applikon, Hyperforma, DynaDrive & XDR) and demonstrated proficiency in all upstream-related operations, including but not limited to cell banking, seed expansion, production, harvest, and clarification
Proven track record with process scale-up and technology transfer, moving from bench scale to pilot and production plant
Experience with technology transfer across different systems, scales, and sites is highly valued
Experience in late-stage process development, characterization and validation is highly valued
Experience in IND and BLA, validation planning, and execution is highly valued
Experience in commercial lifecycle management (commercial process optimizations, comparability, control charting and process capability)
Strong communication, management, and interpersonal skills to effectively influence across the organization and with CDMOs/CMOs
Excellent attention to detail and organizational skills, with a focus on quality and technical excellence
Good information management and data organization skills
Exceptional interpersonal skills with the ability to work individually, within a multi-disciplinary team, as well as with external partners and regulators
A track record of working under pressure and delivering high-quality results to tight deadlines
Summit does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Summit’s Talent Acquisition team at recruiting@smmttx.com to obtain prior written authorization before referring any candidates to Summit.
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Manager, Upstream MSAT employer: Summit Therapeutics Sub, Inc.
Contact Detail:
Summit Therapeutics Sub, Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Manager, Upstream MSAT
✨Tip Number 1
Familiarise yourself with the latest advancements in upstream bioprocessing, especially related to monoclonal antibodies. Being able to discuss recent trends or technologies during your interview can demonstrate your passion and expertise in the field.
✨Tip Number 2
Network with professionals in the biopharmaceutical industry, particularly those involved in MSAT roles. Attend relevant conferences or webinars where you can meet potential colleagues and learn more about the challenges they face, which can help you tailor your approach.
✨Tip Number 3
Prepare to discuss specific examples of your experience with process development and technology transfer. Highlight any successful projects you've led or contributed to, as this will showcase your ability to deliver results in a similar role at Summit.
✨Tip Number 4
Research Summit Therapeutics and their lead asset, Ivonescimab. Understanding their clinical trials and the drug's mechanism can give you an edge in interviews, showing that you're genuinely interested in their work and how you can contribute.
We think you need these skills to ace Manager, Upstream MSAT
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in upstream production and process development. Use specific examples that demonstrate your technical skills and achievements in the biotechnology or pharmaceutical field.
Craft a Compelling Cover Letter: Write a cover letter that connects your background to the role of Manager, Upstream MSAT. Emphasise your experience with bioreactor systems and any previous work with CDMOs, showcasing how you can contribute to Summit's goals.
Highlight Relevant Skills: In your application, clearly outline your skills in process troubleshooting, risk assessment, and technology transfer. Mention any experience with regulatory filings and how you've successfully managed projects in a fast-paced environment.
Show Enthusiasm for the Role: Express your passion for the biotechnology industry and your excitement about working on innovative therapies like Ivonescimab. This can help convey your commitment to the company's mission and values.
How to prepare for a job interview at Summit Therapeutics Sub, Inc.
✨Know Your Biologics
Make sure you have a solid understanding of biologics, especially in relation to upstream processes. Familiarise yourself with the specifics of ivonescimab and its clinical trials, as this will show your genuine interest in the role and the company.
✨Demonstrate Technical Expertise
Be prepared to discuss your technical experience in upstream production and process development. Highlight specific bioreactor systems you've worked with and any successful technology transfers you've managed, as these are crucial for the role.
✨Showcase Problem-Solving Skills
Expect questions that assess your ability to troubleshoot and manage process risks. Prepare examples of past challenges you've faced in upstream processes and how you resolved them, demonstrating your critical thinking and adaptability.
✨Build Relationships
Emphasise your interpersonal skills and ability to work collaboratively with cross-functional teams and external partners. Share experiences where you've successfully built relationships that led to improved project outcomes, as this is key for the Manager role.